Position Title: Supervisor, Production – Manufacturing Compliance (Pharma Manufacturing)

Location: NORTH CAROLINA

Job Type: Full-Time

Work Schedule: Monday to Friday between 6Pm to 6am
Compensation: $90,000 – $100,000 annually

Responsibilities

• Coordinates the execution of the daily/weekly production schedule based upon direction from the area production managers. Oversees the production processes on their assigned shift, working on the production floor to coordinate all relevant production activities.
• Interacts with department management and other functional areas to coordinate all support activities relating to their assigned area.
• Empowers assigned personnel to engage in defining and recommending continuous process improvements,
• Completes thorough deviation investigations in a timely fashion, performing detailed root cause analysis and implementing corrective and preventative actions.
• Assures the compliant application of departmental and company policies and procedures, safety programs, standards and cGMP’s.
• Coordinates staffing for their assigned area of responsibility and assures personnel training is up to date. Develops and executes training and follow-up programs to enhance staff development. Regularly evaluates performance of operations personnel.
• Establishes effective communication methods to provide continuity of information across all operations and shifts.
• Supports product release through the efficient review and completion of production batch records.
• Creates, revises and reviews departmental Standard Operating Procedures.
• Provides production data to managers in support of monthly reports and line efficiency tracking.
• Assumes other duties as assigned by production management.
• All employees are responsible for ensuring the compliance to company documents, programs and activities related to the Health, Safety, Environment, Energy, and Quality Management Systems, as per your roles and responsibilities.

Requirements

• BS/BA degree in Life science or engineering discipline preferred (work experience in lieu of a degree is possible0
• Previous supervisor experience in production/manufacturing environment.
• Proven oral and written communication and proofreading skill required
• Detail orient and proficient computer skills: D Microsoft office software , including Excel, word and Access preferred
• Previous experience in FDA regulated industry preferred (3-5 years).